rs45496696
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs45496696(-;-) |
Make rs45496696(-;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356958 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs45496696 |
dbSNP (classic) | rs45496696 |
ClinGen | rs45496696 |
ebi | rs45496696 |
HLI | rs45496696 |
Exac | rs45496696 |
Gnomad | rs45496696 |
Varsome | rs45496696 |
LitVar | rs45496696 |
Map | rs45496696 |
PheGenI | rs45496696 |
Biobank | rs45496696 |
1000 genomes | rs45496696 |
hgdp | rs45496696 |
ensembl | rs45496696 |
geneview | rs45496696 |
scholar | rs45496696 |
rs45496696 | |
pharmgkb | rs45496696 |
gwascentral | rs45496696 |
openSNP | rs45496696 |
23andMe | rs45496696 |
SNPshot | rs45496696 |
SNPdbe | rs45496696 |
MSV3d | rs45496696 |
GWAS Ctlg | rs45496696 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs45496696(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324735delC |
CLNSRC | |
CLNACC |